「exons」の共起表現一覧(1語右で並び替え)
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The gene contains five | exons and four introns. |
The human GALK1 gene contains 8 | exons and spans approximately 7.3 kb of genomic DNA. |
sists of 2 confirmed promoters (P0 and P1), 16 | exons, and at least 6 enhancers. |
th organisms, the chromosome consists of seven | exons and six introns and non-coding sequence. |
It transcribes a 350 amino acid protein from 9 | exons and 2,010 bps in humans. |
The FXI gene is 23kb in length, has 15 | exons, and is found on chromosome 4q32-35. |
The human AGTR2 gene is composed of three | exons and spans at least 5 kb. |
The gene for CXCL14 contains four | exons and is located on chromosome 5 in humans. |
This gene contains 18 | exons and is located on the X chromosome. |
gene spans more than 150 kb, contains over 80 | exons and encodes a protein of approximately 720 kDa |
e for human CCL11 (scya11) is encoded on three | exons and is located on chromosome 17. |
Apo C4 is a 3.3-kb gene consisting of 3 | exons and 2 introns; it is located 0.5 kb 5' to the |
result from differential usage of two terminal | exons and one of which results from exon deletion. |
The gene for CCL8 is encoded by 3 | exons and is located within a large cluster of CC ch |
n the long arm of chromosome 5, consists of 24 | exons and 23 introns and is over 100kb in size. |
The gene for CXCL5 is encoded on four | exons and is located on human chromosome 4 amongst s |
This gene consists of 4 | exons and its alternative splicing generates multipl |
conserved in their genomic (number and size of | exons) and protein (aa length among species) structu |
erentially methylated region (DMR) at their 5' | exons, and this DMR is commonly found in imprinted g |
Four of the alternate first | exons are considered pseudogenes. |
nce called introns (blue) are removed, and the | exons are joined together to form the final function |
l to that of RORγ, except that the two 5'-most | exons are replaced by an alternative exon, located d |
Exons can include both sequences that code for amino | |
cies, including the number and distribution of | exons, cis-regulatory elements, and transcription st |
The 79 | exons code for a protein of over 3500 amino acid res |
The spliced | exons codes for a protein product is finally cleaved |
1,578 of these unannotated | exons contained stop codons thus not considered pote |
intra-molecular reaction which precisely joins | exons derived from separately transcribed RNAs. |
g gene in humans might be divided into a dozen | exons, each less than two hundred base pairs in leng |
by Walter Gilbert in 1977, in which different | exons either within a gene or between two nonallelic |
but this gene is known to contain at least 34 | exons, and its alternative splicing generates 4 tran |
locus includes thirteen unique alternate first | exons followed by four common exons. |
protein involved in the removal of introns and | exons from strings of messenger RNA; the process tak |
ial form of RNA processing in eukaryotes where | exons from two different primary RNA transcripts are |
Rare read-through transcripts, containing | exons from the PRR5 gene which is located immediatel |
g three different alternative non-coding first | exons have been described. |
iants that contain alternative 5' untranslated | exons have been found. |
sed by splicing to remove introns, leaving the | exons in the mature messenger RNA (mRNA). |
hown 12,291 instances of tandem duplication in | exons in human, fly and worm. |
ss III region on chromosome 6 and comprises 11 | exons interlaced by 10 introns. |
Each of the remaining nine 5′ | exons may be spliced to the four common exons, resul |
Each of the remaining nine 5' | exons may be spliced to the four common exons, resul |
Gilbert suggested that | exons might each encode a single protein domain, est |
eatine kinase has 80% homology with the coding | exons of sarcomeric mitochondrial creatine kinase. |
Some | exons of this gene overlap with some exons from the |
Alternative splicing of two | exons of this gene generates four major splice varia |
y alternative splicing, a process by which the | exons of the RNA produced by transcription of a gene |
t both ends, re-ligating, and leaving just the | exons on either side to be translated into protein. |
The human SMAD3 gene is composed of 9 | exons over 129,339 base pairs. |
gene, compared to members 1-3, encompasses 18 | exons rather than 19 or 20. |
produced further 4,660 unidentified duplicated | exons referred to as unannotated exons. |
e in the genome is divided into several parts ( | exons), separated by non-coding sequences (introns). |
at portion of a gene's DNA or RNA, composed of | exons, that codes for protein. |
PKG-I is encoded by two alternatively spliced | exons that specify for the PKG-Iα and PKG-Iβ isoform |
a 2238-bp coding sequence that consists of 11 | exons that span 25 to 30 kb of genomic DNA and encod |
d C/EBPε and -ζ have respectively two and four | exons that lead in the case of C/EBP ε to four isofo |
The branch site, both | exons, the catalytically essential regions of D5 and |
Within the | exons, there is alternating hydrophobic and Lysine-r |
In this fashion, it would be possible for | exons to essentially be "mixed and matched" to produ |
ers and include numerous alternatively spliced | exons to generate thousands of distinct mRNA transcr |
icing after transcription from DNA allows some | exons to be translated interchangeably, leading to s |
35.1% of the unannotated | exons were found in the EST sequence thus confirming |
and has nine | exons which span 70 kb. |
as well as several extra | exons which may or may not be included in transcript |
NA introns leaving behind the coding sequences | exons, which are then spliced and joined together to |
c deletions and insertions (one or more entire | exons), which are frequent causes of cancers such as |
rsor messenger RNA, it consists exclusively of | exons, with all introns removed. |
exon duplication is defined as duplication of | exons within the same gene to give rise to the subse |
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